Bone and Joint Infections Flashcards

1
Q

Osteomyelitis - Pathogenesis

A
  • A progressive infectious process resulting in inflammatory destruction, bone necrosis and new bone formation
  • Pathogenesis requires high innocula, trauma or foreign material
  • 3 types:
    • Haematogenous
    • Contiguous
    • Diabetic
  • May be acute or chronic (relapsing)
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2
Q

Osteomyelitis - Haematogenous

A
  • Following bacteraemia
  • Escpecially in children
  • Affects metaphyseal area of long bones
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3
Q

Osteomyelitis - Contiguous

A
  • After trauma/surgery or overlying soft-tissue infection
  • Due to direct spread on infection
  • Affects any ages
  • Affects any bones
  • May be associated with foreign bodies:
    • Prostheses
    • Pins
    • Plates
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4
Q

Osteomyelitis - Diabetic

A
  • A consequence of:
    • Reduced vascularity
    • Neuropathic skin changes
    • Decreased local immunity
    • Metabolic disturbance
  • Often associated with foot ulcers
    • Assume osteomyelitis if bone is evident at the base of an ulcer
  • Very hard to treat
  • Progressive spread mans often results in amputation
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5
Q

Osteomyelitis - Signs and Symptoms

A
  • Possible acute symptoms
    • Pain
    • Swelling
    • Overlying inflammation
  • Infants may have few localising signs
  • May be evidence of surgery or trauma
  • Possible chronic signs
    • May be minimal
    • Often a sinus (communiation with skin)
    • Old scars
    • May be acutely inflammed
  • On X-ray
    • Periosteal thickening/elevation
    • Lysis and sclerosis
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6
Q

Osteomyelitis - Investigations

A
  • Investigate
    • Blood cultures
    • FBC
    • CRP
    • Deep tissue swabs from theatres
    • Wound swabs? - may be heavily colonised with skin flora
    • Sinus swabs - NO due to contamination with skin flora
    • Imaging
  • Don’t initate antibiotics until necessary samples are taken
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7
Q

Osteomyelitis - Pathogens

A
  • Most common is Staphlococcus aureus
    • **Adhesin **receptors bind
      • Bone matrix
      • Cartilage - collagen-binding
      • Foreign material - fibronectin-binding
  • Infants
    • Group B Streptococci
    • Staphlococcus aureus
    • E. Coli
  • Children 1-6 years
    • Staphlococcus aureus
    • Streptococcus pyogenes
    • H.influenzae
  • Adults
    • Staphlococcus aureus
    • Staphlococcus epidermis
    • Pseudomonas aeruginosa
    • Gram negatives e.g. E.coli
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8
Q

Septic Arthritis

A
  • Infection of joint space
    • Haematogenous
    • Contiguous
  • Most commonly hip or knee
  • Usually monoarticular
  • Predisposed to if existing:
    • Rhematoid arthritis
    • Joint disease
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9
Q

Septic Arthritis - Pathogenesis

A
  • Synovial membrane is highly vascular
  • Local polymorphonuclear response –>
    • Release of proteolytic enzymes and bacterial toxins
    • Rapid cartilage destruction + joint effusion
    • Drecreased blood supply due to compression of vasculature
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10
Q

Septic Arthritis - Signs and Symptoms

A
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11
Q

Septic Arthritis - Pathogens

A
  • Most commonly *Staphylococcus aureus *or Streptococcus species
  • *Haemophilus influenzae *if much less common since HiB vaccine
  • *Neisseria gonorrhoea *in young adults - !
  • Less commonly Gram-negative infection e.g. Pseudomonas in IVDU
  • 10% of infections are polymicrobial
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12
Q

Reactive Arthritis

A
  • May occur following infectious diarrhoea:
    • Salmonella
    • Campylobacter
    • Yersinia
    • Shigella
  • Following STIs = ‘Reiter’s syndrome’ (+ conjunctivitis, arthritis +/- rash)
    • Chlamydia
    • Gonorrhoea
  • Also may be due to Hepatitis B
  • Bacteria will not be cultured from the joint as arthritis is an inflammatory reaction to infection elsewhere
  • Investigate to confirm diagnosis with:
    • Serology
    • Stool cultures
    • GU swabs
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13
Q

Prosthetic Joint Infection

A
  • Septic arthritis in a prosthetic joint
  • May follow joint replacement
      • Months-years after surgery = late infection
  • Follows 0.5-2% of all joint replacements
  • Symptoms may be mild - joint pain/discomfort
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14
Q

Prosthetic Joint Infection - Pathogenesis

A
  • Early infection usually due to direct inoculation - skin type flora
  • Late infection usually haematogenous
  • Often multiple organisms
  • Leads to a biofilm on the foreign material
    • Thought to be involved in most infections now
    • Compled communities of surface-associated cells in an extracellular matrix
    • Provided physical protection against antibiotics
    • Cells may change phenotype making them less susceptible to treatment
    • Sometimes bacteria stop dividing and become dormant - resistant to abx targeting division
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15
Q

Prosthetic Joint Infection - Diagnosis

A
  • Often difficult
  • Hx & examination
    • Chronic infection fewer signs than acute
  • ESR
  • CRP
  • Isotope scans
  • MC&S of joint aspirate
    • Bacteriological diagnosis important
    • Gram stain of joint fluid has poor sensitivity - culture better
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16
Q

Prosthetic Joint Infection - Conservative Treatment

A
  • Conservative
    • Joint retained
    • Drainage, washout and debridement of joint
    • 6 weeks of antibiotics
    • Risk of missing adherent bacteria to cement/prosthesis if only rely on aspiration for diagnosis
    • Success rate approximately 20% - better in:
      • Early post-op cases when treatment is intiated promptly
        • >80% failure rate if debrided >2 days after symptoms present
      • Avirulent organisms i.e. not Staphylococcus aureus
  • Lifelong suppresive therapy if unfit for surgery
    • 30-60% of patients retain useful joint function
  • Do nothing if elderly or comorbidites and symptoms do not impact on quality of life
17
Q

Prosthetic Joint Infection - Radical Treatment

A
  • Involves removal of prosthesis
    • 1 stage replacement
      • Removal and replacement in same operation
        • Uses antibiotic loaded cement
      • 70-80% success
      • May be suitable for patients unfit for 2 operations
    • 2 stage replacement
      • Removal followed by 6 weeks abx (+/- cement spacer impregnated with abx)
        • Then re-implantation
      • 90-95% success rate
      • May require plastic sugery and skin/muscle flaps
18
Q

Treatment - Bone/Joint Infections

A
  • Seek advice dependent on culture results
  • Combination theapy recommended for PJI and often osteomyelitis
  • Abx course:
    • 2-3 weeks for septic arthritis
    • 4 weeks for paediatric osteomyelitis
    • 6-8+ weeks for adult osteomyelitis and PJI - may need to continue for:
      • Months if prosthesis remains in place
      • Years if infection is persistant and can’t be cured
  • Drainage of effusion/pus is essential
    • Also povides specimen for diagnosis
  • Debridedment of all infected bone material essential in osteomyelitis (except paediatric)
  • Removal of prosthetic joint usually required to clear infection
  • NB - rarely necessary to start antibiotics immediately in patients with PJI or chronic osteomyelitis - get appropriate samples for cultures first
19
Q

Treatment - Bone/Joint Infections: Antibiotics

A
  • Sensitivities:
    • *Staphlococcus aureus - **flucloxacillin + rifampicin *or fusidic acid or gentamycin
    • MRSA - vancomycin + rifampicin or fusidic acid
    • Streptococci - benzypenicillin **or **cefuroxime
    • *Coliforms - *consider ciprofloxacin
    • *Pseudomonas - ciprofloxacin/ceftazidime + gentamycin *initially -** ! **check sensitivities
  • IV vs oral
    • Possible to use oral antibiotics for switch therapy
    • Some e.g. clindamycin or ciprofloxacin can be used as part of combination therapy for long-term treatment
    • **! **- advice important
      • Some oral abx are poorly absorbed from gut e.g. penicillin
      • Some penetrate bone poorly e.g. some cephalosporins
20
Q

Reducing Contamination of Operative Site

A
  • Main sources of contamination
    • Patient skin flora
    • Hands of surgical team
    • Pre-existing infection
    • Airborne from:
      • Skin
      • Mucous membranes
      • Clothing of patient/surgical team